@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP421560.RAMiNferv0Idg0jp8elmfm3NzauUFB8Zcf9bhW1Fm09E4
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP421560.RAMiNferv0Idg0jp8elmfm3NzauUFB8Zcf9bhW1Fm09E4130_head
{
this:
np:hasAssertion
dgn-np:NP421560.RAMiNferv0Idg0jp8elmfm3NzauUFB8Zcf9bhW1Fm09E4130_assertion
;
np:hasProvenance
dgn-np:NP421560.RAMiNferv0Idg0jp8elmfm3NzauUFB8Zcf9bhW1Fm09E4130_provenance
;
np:hasPublicationInfo
dgn-np:NP421560.RAMiNferv0Idg0jp8elmfm3NzauUFB8Zcf9bhW1Fm09E4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP421560.RAMiNferv0Idg0jp8elmfm3NzauUFB8Zcf9bhW1Fm09E4130_assertion
a
np:Assertion
.
dgn-np:NP421560.RAMiNferv0Idg0jp8elmfm3NzauUFB8Zcf9bhW1Fm09E4130_provenance
a
np:Provenance
.
dgn-np:NP421560.RAMiNferv0Idg0jp8elmfm3NzauUFB8Zcf9bhW1Fm09E4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP421560.RAMiNferv0Idg0jp8elmfm3NzauUFB8Zcf9bhW1Fm09E4130_assertion
{
miriam-gene:27319
a
ncit:C16612
.
lld:C0001614
a
ncit:C7057
.
dgn-gda:DGNfec61c6003ede7098c3720eb499b140a
sio:SIO_000628
miriam-gene:27319
,
lld:C0001614
;
a
sio:SIO_001121
.
}
dgn-np:NP421560.RAMiNferv0Idg0jp8elmfm3NzauUFB8Zcf9bhW1Fm09E4130_provenance
{
dgn-np:NP421560.RAMiNferv0Idg0jp8elmfm3NzauUFB8Zcf9bhW1Fm09E4130_assertion
dcterms:description
"[Analysis of differences in the patterns of expression of the various subunits showed the alpha1 signal was strongest in combined cirrhotic motor cortex while the alpha3 and beta3 values were greatest in combined cirrhotic frontal cortex.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:9596562
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP421560.RAMiNferv0Idg0jp8elmfm3NzauUFB8Zcf9bhW1Fm09E4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:10+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}